Evidence map›Paper›PMID 30115983›Full record

ArticleScientific reports2018

Metabolic syndrome status over 2 years predicts incident chronic kidney disease in mid-life adults: a 10-year prospective cohort study.

So Jin Lee, Hun Ju Lee, Hyun Jeong Oh, Taehwa Go, Dae Ryong Kang, Jang Young Kim, Ji Hye Huh

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 24 citations in OpenAlex.

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  13. Semaglutide: Charting New Horizons in GLP-1 Analogue Outcome Studies.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2020
    Review
  14. Article
  15. The emerging role of dyslipidemia in diabetic microvascular complications.Current opinion in endocrinology, diabetes, and obesity · 2020
    Review
  16. [Association of metabolic syndrome with chronic kidney disease in premenopausal and postmenopausal women].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2019
    Article
  17. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

So Jin LeeYonsei University, Wonju College of Medicine, Wonju, Korea.
Hun Ju LeeYonsei University, Wonju College of Medicine, Wonju, Korea.
Hyun Jeong OhYonsei University, Wonju College of Medicine, Wonju, Korea.
Taehwa GoCenter of Biomedical Data Science, Yonsei University, Wonju College of Medicine, Wonju, Korea.
Dae Ryong KangCenter of Biomedical Data Science, Yonsei University, Wonju College of Medicine, Wonju, Korea.
Jang Young KimDepartment of Internal Medicine, Yonsei University, Wonju College of Medicine, Wonju, Korea. kimjang713@gmail.com.
Ji Hye HuhDepartment of Internal Medicine, Yonsei University, Wonju College of Medicine, Wonju, Korea. png1212@yonsei.ac.kr.ORCID 0000-0001-5445-8007
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated whether changes in MetS status over two years modify the 10-year risk of CKD and proteinuria. A prospective cohort study was conducted in 7,251 subjects without CKD at baseline. We categorized subjects according to MetS status over two years: non-MetS (no MetS at either visit), intermittent MetS (positive for MetS at one assessment), and persistent MetS (positive for MetS at two assessments). The hazard ratio (HR) of new-onset CKD over 10-year was calculated using Cox models. During the 10-year follow-up period, 923 (12.7%) developed CKD. Compared to the non-MetS group, the fully adjusted HR for new-onset CKD was the highest in the persistent MetS group (HR, 1.53; 95% CI, 1.23-1.90), followed by the intermittent MetS group (HR, 1.29; 95% CI, 1.04-1.59) (P for trend <0.001). The HR for developing proteinuria was 1.79 (95% CI, 1.15-2.79) in the persistent MetS group and 0.70 (95% CI, 0.42-1.19) in the intermittent MetS group when the non-MetS group was considered as the reference group. Temporal changes in MetS status over two years influenced the 10-year risk of incident CKD and proteinuria. Our findings suggest that monitoring and strictly controlling MetS are important in preventing renal function decline.

Indexed as

Cohort StudiesFemaleHumansIncidenceKaplan-Meier EstimateMaleMetabolic SyndromeMiddle AgedPrognosisProspective StudiesProteinuriaRenal Insufficiency, ChronicRisk Factors

Identifiers

PMID30115983
PMCPMC6095861
OpenAlexW2887335350

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.